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Gmp Consulting Jobs (NOW HIRING)

Techtrueup

Machine Operator (GMP)- 2nd shift

Clinton, PA · On-site

$16.75 - $20/hr

Our wide network of consultants and contract-to-hire engineers brings deep expertise across ... The GMP Associate I supports the manufacturing of high-quality medical devices by operating ...

Pace

PLS GMP Manufacturing Technician I

Norristown, PA · On-site

$22 - $28/hr

This is a full-time, onsite, GMP Manufacturing Technician (Solid Dose) position located in ... consulting, and facility support services to the pharmaceutical, biopharmaceutical, and gene ...

GMP Pros

Technical Sales Representative

Omaha, NE · On-site

$100/hr

If that's you - GMP Pros wants to hear from you. Who We Are GMP Pros, Inc. ® is a fast-growing ... the consultative polish of an account manager who earns trust in a complex, regulated industry.

AbbVie

GMP Utility Engineer

Worcester, MA · On-site

Serve as subject matter expert for GMP utilities at ABC, including support for audits, regulatory ... Oversee design work of internal and external consultants, Creates/modified designs for intermediate ...

AbbVie

GMP Utility Engineer

Worcester, MA · On-site

$84K/yr

Serve as subject matter expert for GMP utilities at ABC, including support for audits, regulatory ... Oversee design work of internal and external consultants, Creates/modified designs for intermediate ...

AbbVie

GMP Utility Engineer

Worcester, MA

Serve as subject matter expert for GMP utilities at ABC, including support for audits, regulatory ... Oversee design work of internal and external consultants, Creates/modified designs for intermediate ...

Eliquent Life Sciences, Inc

Consultant 1

Montrose, CA · On-site

Knowledge of GMP, GAMP 5, 21 CFR Part 11, EU Annex 11 * Strong documentation, communication, and organizational skills * Ability to work independently and within cross-functional teams * Consulting ...

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How much do gmp consulting jobs pay per hour?

As of Jul 24, 2026, the average hourly pay for gmp consulting in the United States is $17.79, according to ZipRecruiter salary data. Most workers in this role earn between $17.07 and $18.51 per hour, depending on experience, location, and employer.

What are common challenges faced by consultants working in GMP (Good Manufacturing Practice) consulting roles?

Consultants in GMP consulting often face challenges such as staying current with evolving regulatory requirements, adapting to different client company cultures, and managing multiple projects with tight deadlines. They must quickly assess manufacturing processes, identify compliance gaps, and clearly communicate solutions to clients who may have varying levels of GMP knowledge. Effective collaboration with cross-functional teams and the ability to provide practical, actionable advice are key to overcoming these challenges and ensuring successful project outcomes.

What is GMP consulting?

GMP consulting refers to professional services that help companies comply with Good Manufacturing Practice (GMP) regulations in industries like pharmaceuticals, food, and cosmetics. GMP consultants provide expertise in interpreting regulatory standards, preparing for inspections, developing quality management systems, and ensuring manufacturing processes meet legal and safety requirements. Their goal is to help businesses maintain compliance, improve product quality, and avoid costly regulatory issues.

What is the difference between Gmp Consulting vs Quality Assurance Specialist?

AspectGmp ConsultingQuality Assurance Specialist
CredentialsGMP certifications, industry-specific trainingGMP certifications, QA certifications
Work EnvironmentConsulting firms, client sites, regulatory agenciesPharmaceutical, biotech companies, manufacturing facilities
Employer & IndustryConsulting firms, pharma, biotechPharmaceutical companies, biotech firms
Search & Comparison IntentYesYes

Gmp Consulting professionals provide expert advice on GMP compliance, often working across multiple client sites, while Quality Assurance Specialists focus on maintaining quality standards within a specific organization. Both roles require GMP knowledge and certifications but differ in scope and work environment.

What are the key skills and qualifications needed to thrive as a GMP Consultant, and why are they important?

To excel as a GMP Consultant, you need a deep understanding of Good Manufacturing Practices, regulatory compliance, and quality assurance, typically backed by a degree in life sciences or engineering. Familiarity with industry-specific regulations (such as FDA or EMA guidelines), quality management systems (QMS), and relevant certifications like Six Sigma or ASQ-CQA is highly valuable. Strong analytical thinking, communication skills, and attention to detail are essential for effectively advising clients and implementing compliance solutions. These competencies ensure that organizations meet regulatory standards, minimize risk, and maintain product quality.
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What states have the most Gmp Consulting jobs? States with the most job openings for Gmp Consulting jobs include:
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Gmp Consulting jobs near you
Infographic showing various Gmp Consulting job openings in the United States as of July 2026, with employment types broken down into 92% Full Time, 4% Part Time, and 4% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $37,000 per year, or $17.8 per hour.
Machine Operator (GMP)- 2nd shift

Machine Operator (GMP)- 2nd shift

Techtrueup

Clinton, PA • On-site

$16.75 - $20/hr

Contractor

Posted 18 days ago

Job description

Company Description
Fusion Life Sciences Technologies (www.fusionlifesolutions.com ) is a WBE-certified Healthcare Staffing and Engineering Services provider supporting industries including Pharma, Medical Devices, Aeronautical, Supply Chain, Heavy/Light Industrial, Food & Beverage, and Automotive. We proudly partner with 120+ clients such as Johnson & Johnson, Haemonetics, Delta, Caterpillar, Artisan Chef, Baxter, and many more. Our wide network of consultants and contract-to-hire engineers brings deep expertise across Engineering, Technical, Administrative, Healthcare, Life Sciences, Blue Collar, Skilled Trades, IT, Software Development, Manufacturing, and Supply Chain sectors. What sets us apart is our AI-powered, in-house software's enabling us to source and screen top talent within hours. This ensures rapid response times, high-quality matches, and virtually zero attrition.
Job Description
Job Title : GMP Associate I - 2nd shift
Duration : 6 Months
Location : Clinton, PA
Summary:
The GMP Associate I supports the manufacturing of high-quality medical devices by operating equipment, packing finished products, loading automatic hoppers, and resolving basic equipment faults through HMI (Human-Machine Interface) screens. This role requires adherence to Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and cleanroom standards while contributing to a safe, lean, and team-oriented environment.
Key Responsibilities
1. Safety
• Follow all safety procedures, including the proper use of PPE.
• Report hazards, malfunctions, and incidents promptly.
2. Quality
• Adhere to cleanroom protocols and gowning requirements.
• Maintain accurate, compliant documentation (batch records, logs, GDP).
• Perform in-process checks and follow GMP, FDA, and ISO 13485 standards.
3. Manufacturing & Delivery
• Load hoppers and monitor material levels to avoid interruptions.
• Assemble components and subassemblies per work instructions.
• Execute activities in molding such as proper packaging and completion of GDP paperwork.
• Operate production equipment and resolve basic HMI faults, escalating as needed.
• Perform routine cleaning and sanitization of equipment and workspace.
4. Continuous Improvement
• Participate in lean initiatives (5S, Kaizen, QEK).
• Complete required lean curriculum for associate level.
5. Company Values
• Collaborate with Quality, Engineering, and other teams to achieve production goals.
• Uphold company values and policies with professionalism.
• Stand for extended periods; perform repetitive tasks.
• Lift/move up to 25 lbs as needed.
• Wear cleanroom attire (gown, mask, gloves) for prolonged periods.
Qualifications
• High school diploma or equivalent.
• Prior manufacturing or production experience preferred.
• Basic knowledge of HMI systems and cleanroom procedures a plus.
• Strong attention to detail and commitment to quality.
• Ability to stand for long periods and perform repetitive tasks.
• Willingness to wear full cleanroom PPE.
Physical Requirements
• Stand for extended periods; perform repetitive motions.
• Lift/move up to 25 lbs as needed.
• Wear cleanroom attire (gown, mask, gloves) for prolonged periods.
Qualifications
Additional Information
All your information will be kept confidential according to EEO guidelines.

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